Canonical Allele Identifier: CA382706501

Gene: APOA4

Linked Data

• MyVariant Identifiers: chr11:g.116693483C>A (hg19) ; chr11:g.116822767C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116822767C>A , CM000673.2:g.116822767C>A	GRCh38
NC_000011.9:g.116693483C>A , CM000673.1:g.116693483C>A	GRCh37
NC_000011.8:g.116198693C>A	NCBI36
NG_012044.1:g.5529G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357780.5:c.68G>T MANE Select	ENSP00000350425.3:p.Ser23Ile
ENST00000357780.4:c.68G>T	ENSP00000350425.3:p.Ser23Ile
NM_000482.3:c.68G>T	NP_000473.2:p.Ser23Ile
NM_000482.4:c.68G>T MANE Select	NP_000473.2:p.Ser23Ile